(1897801), N. A., (11704868), S. W., (496764), L. R., (18527778), R. J. v. H., (311778), S. H. R., & (18508167), O. M. A. (2021). Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.
توثيق أسلوب شيكاغو (الطبعة السابعة عشر)(1897801), Nerea Alonso, Sachin Wani (11704868), Lorraine Rose (496764), Rob J. van't Hof (18527778), Stuart H. Ralston (311778), و Omar M.E. Albagha (18508167). Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice. 2021.
توثيق جمعية اللغة المعاصرة MLA (الإصدار التاسع)(1897801), Nerea Alonso, et al. Insertion Mutation in Tnfrsf11a Causes a Paget's Disease–Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice. 2021.